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d-Tartaric acid

Base Information Edit
  • Chemical Name:d-Tartaric acid
  • CAS No.:147-71-7
  • Deprecated CAS:1150316-16-7
  • Molecular Formula:C4H6O6
  • Molecular Weight:150.088
  • Hs Code.:29181200
  • European Community (EC) Number:205-695-6
  • ICSC Number:0772
  • UNII:RRX6A4PL3C
  • DSSTox Substance ID:DTXSID4043775,DTXSID5046986
  • Nikkaji Number:J9.264I
  • Wikipedia:Tartaric acid,Tartaric_acid,Tartrate
  • Wikidata:Q23034947
  • NCI Thesaurus Code:C47744
  • RXCUI:37578
  • Metabolomics Workbench ID:44098
  • ChEMBL ID:CHEMBL1200861
  • Mol file:147-71-7.mol
d-Tartaric acid

Synonyms:(R*,R*)-(+-)-2,3-dihydroxybutanedioic acid, monoammonium monosodium salt;aluminum tartrate;ammonium tartrate;calcium tartrate;calcium tartrate tetrahydrate;Mn(III) tartrate;potassium tartrate;seignette salt;sodium ammonium tartrate;sodium potassium tartrate;sodium tartrate;stannous tartrate;tartaric acid;tartaric acid, ((R*,R*)-(+-))-isomer;tartaric acid, (R*,S*)-isomer;tartaric acid, (R-(R*,R*))-isomer;tartaric acid, (S-(R*,R*))-isomer;tartaric acid, ammonium sodium salt, (1:1:1) salt, (R*,R*)-(+-)-isomer;tartaric acid, calcium salt, (R-R*,R*)-isomer;tartaric acid, monoammonium salt, (R-(R*,R*))-isomer;tartrate

Suppliers and Price of d-Tartaric acid
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • D-(?)-Tartaric acid
  • 50g
  • $ 80.00
  • TCI Chemical
  • D-(-)-Tartaric Acid >99.0%(T)
  • 100g
  • $ 120.00
  • TCI Chemical
  • D-(-)-Tartaric Acid >99.0%(T)
  • 500g
  • $ 260.00
  • TCI Chemical
  • D-(-)-Tartaric Acid >99.0%(T)
  • 25g
  • $ 39.00
  • SynQuest Laboratories
  • D-(-)-Tartaric acid 99%
  • 25 g
  • $ 20.00
  • SynQuest Laboratories
  • D-(-)-Tartaric acid 99%
  • 100 g
  • $ 61.00
  • SynQuest Laboratories
  • D-(-)-Tartaric acid 99%
  • 500 g
  • $ 152.00
  • Sigma-Aldrich
  • D-(?)-Tartaric acid puriss., unnatural form, ≥99.0% (T)
  • 250g
  • $ 416.00
  • Sigma-Aldrich
  • Tartaric acid United States Pharmacopeia (USP) Reference Standard
  • 1 g
  • $ 414.00
  • Sigma-Aldrich
  • (2S,3S)-(-)-Tartaric acid for the resolution of racemates for synthesis. CAS 147-71-7, chemical formula HOOCCH(OH)CH(OH)COOH., for the resolution of racemates for synthesis
  • 8007990100
  • $ 192.00
Total 240 raw suppliers
Chemical Property of d-Tartaric acid Edit
Chemical Property:
  • Appearance/Colour:white crystals 
  • Vapor Pressure:4.93E-08mmHg at 25°C 
  • Melting Point:172-174 °C(lit.) 
  • Refractive Index:-12.5 ° (C=5, H2O) 
  • Boiling Point:399.3 °C at 760 mmHg 
  • PKA:3.0, 4.4(at 25℃) 
  • Flash Point:209.4 °C 
  • PSA:115.06000 
  • Density:1.886 g/cm3 
  • LogP:-2.12260 
  • Storage Temp.:Store below +30°C. 
  • Sensitive.:Light Sensitive 
  • Solubility.:water: soluble100mg/mL, clear, colorless 
  • Water Solubility.:1394 g/L (20 ºC) 
  • XLogP3:-1.9
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:150.01643791
  • Heavy Atom Count:10
  • Complexity:134
Purity/Quality:

99.5%, *data from raw suppliers

D-(?)-Tartaric acid *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36/37-37/39-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Other Classes -> Organic Acids
  • Canonical SMILES:C(C(C(=O)O)O)(C(=O)O)O
  • Isomeric SMILES:[C@H]([C@@H](C(=O)O)O)(C(=O)O)O
  • Recent NIPH Clinical Trials:Unraveling of neural basis of voluntary cough and cough reflex
  • Inhalation Risk:Evaporation at 20 °C is negligible; a harmful concentration of airborne particles can, however, be reached quickly when dispersed.
  • Effects of Short Term Exposure:Corrosive. The substance is corrosive to the eyes, skin and respiratory tract. Corrosive on ingestion. Inhalation of the aerosol may cause lung oedema. The effects may be delayed. Medical observation is indicated.
  • Uses D-(-)-Tartaric Acid the synthetic enantiomer of L-(+)-Tartaric Acid (T007630), used in the preparation of synthetic analgesics. tartaric acid is the second largest AHA in size (glycolic acid being the smallest AHA and citric acid the largest). It is not frequently used in cosmetic or anti-aging preparations as formulators find it difficult to work with and it can cause irritation to the skin. Tartaric Acid is an acidulant that occurs naturally in grapes. It is hygroscopic and rapidly soluble, with a solubility of 150 g in 100 ml of distilled water at 25°c. It has a slightly tarter taste than citric acid, with a tartness equivalent of 0.8–0.9. It augments the flavor of fruits in which it is a natural constituent. It is used in grapeand limeflavored beverages and grape-flavored jellies. It is used as an acidulant in baking powder and as a synergist with antioxidants to prevent rancidity. D-(-)-Tartaric acid is used as a resolving agent in organic synthesis. It is used as a precursor for the preparation of its ester derivatives like D-tartaric acid diethyl ester, D-tartaric acid dimethyl ester and D-tartaric acid diiso-propyl ester. It finds application in the synthesis of chiral aziridine derivative, a common intermediate for the preparation of hydroxyethylamine class HIV protease inhibitors viz. as saquinavir, amprenavir and nelfinavir. It is widely used in the food industry as a beer foaming agent, for food acidity regulations and as a flavoring agent.
Technology Process of d-Tartaric acid

There total 53 articles about d-Tartaric acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With water; sodium hydroxide; In N,N-dimethyl-formamide; at 60 ℃; for 10h; Time;
Guidance literature:
With sulfuric acid; In ethanol; at 20 ℃; for 0.75h;
Guidance literature:
With hydrogenchloride; ammonia; In water; ethyl acetate; at 70 ℃; for 6h; pH=5 - 11;
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